Zobrazeno 1 - 3
of 3
pro vyhledávání: '"physiopathology [Deglutition Disorders]"'
Autor:
Sebastian Contreras Cubillos, Roberto Rodríguez-Labrada, Matthis Synofzik, Tamara Canento, Winfried Ilg, Jacqueline Medrano-Montero, Yaimeé Vázquez-Mojena, Sandra Rojas, Luis Velázquez-Pérez, Melissa P. Cyngler, Fernanda Maldonado, Reidenis Torres-Vega, Megan Kruse, Michelle Magee, Adam P. Vogel
Publikováno v:
Neurology 95(2), e194-e205 (2020). doi:10.1212/WNL.0000000000009776
ObjectiveTo determine whether objective and quantitative assessment of dysarthria and dysphagia in spinocerebellar ataxia type 2 (SCA2), specifically at pre-ataxic and early disease phases, can act as sensitive disease markers.MethodsForty-six indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d9e92e7d850a0306866ec288f2d1780
https://doi.org/10.1212/wnl.0000000000009776
https://doi.org/10.1212/wnl.0000000000009776
Autor:
Rafał Rola, Antonella Antenora, Tanja Schmitz-Hübsch, Massimo Pandolfo, Bart P.C. van de Warrenburg, Anna Castaldo, Alexis Brice, Wolfgang Nachbauer, Sophie Tezenas du Montcel, José Berciano, Arron Cook, Paola Giunti, Caterina Mariotti, Jörg B. Schulz, Lorenzo Nanetti, Heike Jacobi, Kang Jun-Suk, Jon Infante, Holger Hengel, Alexandra Durr, Laszlo Baliko, Thomas Klockgether, Ludger Schöls, Michael H Parkinson, Alessandro Filla, Béla Melegh, Maria Rakowicz, Alhassane Diallo, Perrine Charles, Sylvia Boesch, Anna Sulek, Dagmar Timmann, Peter Bauer, Cecila Marelli, Robyn Labrum, Marta Panzeri
Publikováno v:
Movement disorders
Movement disorders 34(8), 1220-1227 (2019). doi:10.1002/mds.27739
Movement Disorders, 34, 1220-1227
Movement Disorders, 34, 8, pp. 1220-1227
Movement disorders 34(8), 1220-1227 (2019). doi:10.1002/mds.27739
Movement Disorders, 34, 1220-1227
Movement Disorders, 34, 8, pp. 1220-1227
Background: Spinocerebellar ataxias are rare dominantly inherited neurodegenerative diseases that lead to severe disability and premature death. Objective: To quantify the impact of disease progression measured by the Scale for the Assessment and Rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2527d82655eeffa347c74770eb8a24d5
https://www.ncbi.nlm.nih.gov/pubmed/31211461
https://www.ncbi.nlm.nih.gov/pubmed/31211461
Autor:
Dagmar Timmann, Natalie Rommel, Adam P. Vogel, Eva-Maria Kraus, Elsdon Storey, Patrick Krumm, Cynthia Gagnon, Ludger Schöls, Marius Horger, Andreas Oettinger, Lisa H. Stoll, Matthis Synofzik
Publikováno v:
Journal of neurology 265(9), 2060-2070 (2018). doi:10.1007/s00415-018-8950-4
Autosomal recessive spastic ataxia of Charlevoix–Saguenay (ARSACS) is a rare early onset neurodegenerative disease that typically results in ataxia, upper motor neuron dysfunction and sensorimotor peripheral neuropathy. Dysarthria and dysphagia are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::465b3270602ecf67ab3c01466c94514e
https://pub.dzne.de/record/140167
https://pub.dzne.de/record/140167